chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241510092241510092G4GENIChomozygous127497415
1241510095241510095T4GENIChomozygous127497416
1241510097241510097G3GENIChomozygous127497417
1241510184241510184T5GENIChomozygous127497419
1241510194241510194C6GENIChomozygous127497420
1241510231241510232AG17GENIChomozygous120476557
1241510232241510233GA17GENIChomozygous120476558
1241510266241510266G20GENIChomozygous127497421
1241510274241510275C21GENIChomozygous127497422
1241510280241510280T20GENIChomozygous127497423
1241510293241510293G20GENIChomozygous127497424
1241510316241510316G18GENIChomozygous127497425
1241510317241510317T18GENIChomozygous127497426
1241510328241510328C14GENIChomozygous127497427
1241515200241515200G6GENIChomozygous127497428
1241529610241529642GACACAAAAAATAGTTGTCATCATAAACAAAG20GENIChomozygous127497429
1241531764241531765G4GENIChomozygous127497430
1241531791241531792C4GENIChomozygous127497431
1241531826241531826C2GENIChomozygous127497432
1241531828241531829GC2GENIChomozygous121201882